Eckhardt Christina M, Wu Haotian, Jackson Gabriela, Sobel Marisa H, Bloomquist Tessa, Divjan Adnan, da Silva Hadler, Best Lyle G, Cole Shelley, Umans Jason, Zhang Ying, de Hoff Peter, Laurent Louise C, Perzanowski Matthew S, Cheng Ke, Baccarelli Andrea A, Sanchez Tiffany R
Division of Pulmonary, Allergy and Critical Care Medicine, Department of Medicine, Columbia University Vagelos College of Physicians and Surgeons, New York, NY; Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY.
Department of Environmental Health Sciences, Columbia University Mailman School of Public Health, New York, NY.
Chest. 2025 Jan;167(1):87-97. doi: 10.1016/j.chest.2024.08.004. Epub 2024 Aug 16.
American Indian populations have experienced marked disparities in respiratory disease burden. Extracellular vesicle-encapsulated microRNAs (EV-miRNAs) are a novel class of biomarkers that may improve recognition of lung damage in indigenous populations in the United States.
Are plasma EV-miRNAs viable biomarkers of respiratory health in American Indian populations?
The Strong Heart Study is a prospective cohort study that enrolled American Indian patients aged 45 to 74 years. EV-miRNA expression was measured in plasma (1993-1995). Respiratory health outcomes, including prebronchodilator FEV, FVC, and respiratory symptom burden, were ascertained in the same study visit. Club cell secretory protein (CC-16), an antiinflammatory pneumoprotein implicated in COPD pathogenesis, was measured in serum. Linear and logistic regression were used for statistical analyses. Biological pathway analyses were used to elucidate gene targets of significant EV-miRNAs.
Among 853 American Indian adults, three EV-miRNAs were associated with FEV, four EV-miRNAs were associated with FVC, and one EV-miRNA was associated with FEV/FVC (P < .05). Increased miR-1294 expression was associated with higher odds of airflow limitation (OR, 1.29; 95% CI, 1.07-1.55), whereas increased expression of miR-1294 (OR, 1.32; 95% CI, 1.07-1.63) and miR-532-5p (OR, 1.57; 95% CI, 1.02-2.40) was associated with higher odds of restriction. Increased miR-451a expression was associated with lower odds of exertional dyspnea (OR, 0.71; 95% CI, 0.59-0.85). Twenty-two EV-miRNAs were associated with serum CC-16 levels (q < 0.05), suggesting that EV-miRNAs may play a role in the pathway linking CC-16 to COPD pathogenesis. A pathway analysis showed key EV-miRNAs targeted biological pathways that modulate inflammation, immunity, and structural integrity in the lungs.
Circulating EV-miRNAs are novel mechanistic biomarkers of respiratory health and may facilitate the early detection and treatment of lung damage in American Indian populations that have been disproportionately affected by chronic lung diseases.
美国印第安人群在呼吸道疾病负担方面存在显著差异。细胞外囊泡包裹的微小RNA(EV-miRNAs)是一类新型生物标志物,可能有助于提高对美国本土人群肺损伤的识别。
血浆EV-miRNAs是否是美国印第安人群呼吸道健康的可行生物标志物?
强心研究是一项前瞻性队列研究,纳入了年龄在45至74岁的美国印第安患者。在血浆中测量EV-miRNA表达(1993 - 1995年)。在同一次研究访视中确定呼吸道健康结局,包括支气管扩张剂前FEV、FVC和呼吸道症状负担。在血清中测量俱乐部细胞分泌蛋白(CC - 16),这是一种与慢性阻塞性肺疾病(COPD)发病机制有关的抗炎肺蛋白。采用线性和逻辑回归进行统计分析。使用生物通路分析来阐明显著EV-miRNAs的基因靶点。
在853名美国印第安成年人中,三种EV-miRNAs与FEV相关,四种EV-miRNAs与FVC相关,一种EV-miRNA与FEV/FVC相关(P < 0.05)。miR - 1294表达增加与气流受限几率较高相关(比值比[OR],1.29;95%置信区间[CI],1.07 -